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Clinical outcomes among unresectable, locally advanced, and metastatic cutaneous squamous cell carcinoma patients treated with systemic therapy

机译:通过全身治疗治疗的不可切除,局部晚期和转移皮肤鳞状细胞癌患者的临床结果

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Prior studies of conventional chemotherapy or epidermal growth factor receptor inhibitors for advanced (ie, locally advanced cutaneous squamous cell carcinoma [laCSCC] or metastatic [mCSCC]) cutaneous squamous cell cancer enrolled?≤?40 patients. This retrospective, observational study assessed real‐world treatment patterns and clinical outcomes in patients with unresectable laCSCC or mCSCC using electronic health records of patients who initiated first‐line (1L) systemic treatment from 1 January 2008 to 31 December 2015, with follow‐up to 30 September 2017. The median duration of follow‐up from 1L treatment was 10.1?months (range 0.03‐67.6?months). Duration of therapy (DOT) and overall survival (OS) were assessed using Kaplan‐Meier analysis. Response rate was calculated as the proportion of patients who achieved physician‐assessed‐response. Eighty‐two patients were identified (17 laCSCC and 65 mCSCC). Median age at 1L treatment initiation was 75?years; 85% were male, 88% had an Eastern Cooperative Oncology Group performance status of 1, and 84% had received radiotherapy. The most common 1L regimens were carboplatin?+?paclitaxel (27%) and cetuximab monotherapy (24%). The median 1L DOT was 4.1?months for laCSCC and 2.3?months for mCSCC. The physician‐assessed response rate for 1L therapy was 17.6% for laCSCC, and 18.5% for mCSCC. The median OS from 1L treatment initiation was 16.2?months for laCSCC, and 15.3?months for mCSCC. Only 24 patients (29%) received second‐line therapy. This is the largest retrospective data set regarding patients with advanced CSCC treated with anticancer systemic therapy prior to approval of the anti‐programmed cell death‐1 antibody, cemiplimab. Efficacy was low in both laCSCC and mCSCC. These data provide historic benchmarks for outcomes in patients with advanced CSCC prior to Food and Drug Administration approval of cemiplimab‐rwlc.
机译:对先进的常规化疗或表皮生长因子受体抑制剂的先前研究(即局部先进的皮肤鳞状细胞癌[LACSCC]或转移[MCSCC])注册的皮肤鳞状细胞癌?≤20例。这种回顾性的观察性研究评估了利用2008年1月1日至2015年12月31日从2008年1月1日开始的第一线(1L)全身治疗的患者的电子健康记录,评估了患者的现实治疗模式和临床结果。到2017年9月30日。1L治疗中随访的中位持续时间为10.1?月(范围0.03-67.6?月)。使用Kaplan-Meier分析评估治疗持续时间(点)和总存活(OS)。响应率计算为达到医生评估响应的患者的比例。鉴定了八十二名患者(17LACSCC和65 MCSCC)。 1L治疗开始的中位年龄为75岁;年龄; 85%是男性,88%的东部合作肿瘤学组绩效地位为1,84%已收到放射疗法。最常见的1L方案是Carboplatin?+?紫杉醇(27%)和西妥昔单抗单药治疗(24%)。中位数1L点为4.1个月,Lacscc和2.3个月为MCSCC。对于LACSCC的1L疗法的医生评估的反应率为17.6%,MCSCC为18.5%。来自1L治疗开始的中位OS为LACSCC为16.2个月,MCSCC为15.3个月。只有24名患者(29%)接受了二线治疗。这是关于在批准反编程的细胞死亡-1抗体,Cemimplimab之前,有关患有抗癌系统治疗的先进CSCC治疗患者的最大回顾性数据集。 LACSCC和MCSCC效力低。这些数据为在食品和药物管理局批准的CeMiplimab-RWLC批准之前提供了高级CSCC患者的结果的历史基准。

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